Linked Data
ClinVar Variation Id:
14542
ClinVar RCV Id:
RCV000015643
dbSNP Id:
rs786205094
gnomAD v4:
1-209630653-CA-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.209630654del , CM000663.2:g.209630654del | GRCh38 |
| NC_000001.10:g.209803999del , CM000663.1:g.209803999del | GRCh37 |
| NC_000001.9:g.207870622del | NCBI36 |
| NG_007116.1:g.26822del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356082.9:c.904del MANE Select | ENSP00000348384.3:p.Trp302GlyfsTer? | |
| ENST00000356082.8:c.904del | ENSP00000348384.3:p.Trp302GlyfsTer? | |
| ENST00000367030.7:c.904del | ENSP00000355997.3:p.Trp302GlyfsTer? | |
| ENST00000391911.5:c.904del | ENSP00000375778.1:p.Trp302GlyfsTer? | |
| NM_000228.2:c.904del | NP_000219.2:p.Trp302GlyfsTer? | |
| NM_001017402.1:c.904del | NP_001017402.1:p.Trp302GlyfsTer? | |
| NM_001127641.1:c.904del | NP_001121113.1:p.Trp302GlyfsTer? | |
| XM_005273124.3:c.904del | XP_005273181.1:p.Trp302GlyfsTer? | |
| XM_005273124.4:c.904del | XP_005273181.1:p.Trp302GlyfsTer? | |
| XM_017001272.2:c.712del | XP_016856761.1:p.Trp238GlyfsTer? | |
| NM_000228.3:c.904del MANE Select | NP_000219.2:p.Trp302GlyfsTer? | |
| NM_001017402.2:c.904del | NP_001017402.1:p.Trp302GlyfsTer? |